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Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial
Background: We investigated whether Neuron-specific enolase (NSE) serum concentration predicts long-term mortality and poor neurological outcome in adult cardiac arrest patients. Methods: Within this prospective observational study, we included consecutive adult patients admitted to the intensive ca...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8624292/ https://www.ncbi.nlm.nih.gov/pubmed/34822369 http://dx.doi.org/10.3390/medicines8110072 |
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author | Müller, Jonas Bissmann, Benjamin Becker, Christoph Beck, Katharina Loretz, Nina Gross, Sebastian Amacher, Simon A. Bohren, Chantal Pargger, Hans Tisljar, Kai Sutter, Raoul Marsch, Stephan Hunziker, Sabina |
author_facet | Müller, Jonas Bissmann, Benjamin Becker, Christoph Beck, Katharina Loretz, Nina Gross, Sebastian Amacher, Simon A. Bohren, Chantal Pargger, Hans Tisljar, Kai Sutter, Raoul Marsch, Stephan Hunziker, Sabina |
author_sort | Müller, Jonas |
collection | PubMed |
description | Background: We investigated whether Neuron-specific enolase (NSE) serum concentration predicts long-term mortality and poor neurological outcome in adult cardiac arrest patients. Methods: Within this prospective observational study, we included consecutive adult patients admitted to the intensive care unit (ICU) after cardiac arrest. NSE was measured upon ICU admission and on days 1, 2, 3, 5 and 7. Results: Of 403 patients, 176 (43.7%) survived. Median follow-up duration was 43.7 months (IQR 14.3 to 63.0 months). NSE levels on day 3 were increased more than threefold in non-survivors compared to survivors (median NSE (ng/mL) 19.8 (IQR 15.7 to 27.8) vs. 72.6 (IQR 26 to 194)) and showed the highest prognostic performance for mortality compared to other days of measurement, with an AUC of 0.81 and an adjusted hazard ratio of 1.55 (95% CI 1.41 to 1.71, p < 0.001). Subgroup analysis showed an excellent sensitivity and negative predictive value of 100% of NSE in patients <54 years of age. Conclusion: NSE measured three days after cardiac arrest is associated with long-term mortality and neurological outcome and may provide prognostic information that improves clinical decision making. Particularly in the subgroup of younger patients (<54 years), NSE showed excellent negative predictive value. |
format | Online Article Text |
id | pubmed-8624292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86242922021-11-27 Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial Müller, Jonas Bissmann, Benjamin Becker, Christoph Beck, Katharina Loretz, Nina Gross, Sebastian Amacher, Simon A. Bohren, Chantal Pargger, Hans Tisljar, Kai Sutter, Raoul Marsch, Stephan Hunziker, Sabina Medicines (Basel) Article Background: We investigated whether Neuron-specific enolase (NSE) serum concentration predicts long-term mortality and poor neurological outcome in adult cardiac arrest patients. Methods: Within this prospective observational study, we included consecutive adult patients admitted to the intensive care unit (ICU) after cardiac arrest. NSE was measured upon ICU admission and on days 1, 2, 3, 5 and 7. Results: Of 403 patients, 176 (43.7%) survived. Median follow-up duration was 43.7 months (IQR 14.3 to 63.0 months). NSE levels on day 3 were increased more than threefold in non-survivors compared to survivors (median NSE (ng/mL) 19.8 (IQR 15.7 to 27.8) vs. 72.6 (IQR 26 to 194)) and showed the highest prognostic performance for mortality compared to other days of measurement, with an AUC of 0.81 and an adjusted hazard ratio of 1.55 (95% CI 1.41 to 1.71, p < 0.001). Subgroup analysis showed an excellent sensitivity and negative predictive value of 100% of NSE in patients <54 years of age. Conclusion: NSE measured three days after cardiac arrest is associated with long-term mortality and neurological outcome and may provide prognostic information that improves clinical decision making. Particularly in the subgroup of younger patients (<54 years), NSE showed excellent negative predictive value. MDPI 2021-11-17 /pmc/articles/PMC8624292/ /pubmed/34822369 http://dx.doi.org/10.3390/medicines8110072 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Müller, Jonas Bissmann, Benjamin Becker, Christoph Beck, Katharina Loretz, Nina Gross, Sebastian Amacher, Simon A. Bohren, Chantal Pargger, Hans Tisljar, Kai Sutter, Raoul Marsch, Stephan Hunziker, Sabina Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial |
title | Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial |
title_full | Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial |
title_fullStr | Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial |
title_full_unstemmed | Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial |
title_short | Neuron-Specific Enolase (NSE) Predicts Long-Term Mortality in Adult Patients after Cardiac Arrest: Results from a Prospective Trial |
title_sort | neuron-specific enolase (nse) predicts long-term mortality in adult patients after cardiac arrest: results from a prospective trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8624292/ https://www.ncbi.nlm.nih.gov/pubmed/34822369 http://dx.doi.org/10.3390/medicines8110072 |
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